solute carrier family 25 member 10

Summary
Gene Symbol
  • SLC25A10
Organism
Homo sapiens (human)
External Links
NCBI Gene
1468
PubChem
1468
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Antiport
  • Disease variant
  • Lipid transport
  • Mitochondrion inner membrane
  • Primary mitochondrial disease
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Transmembrane
  • Transmembrane helix
  • Transport
Proteins
Displaying all 4 entries
UniProt Protein Name
A0A0S2Z382
Q9UBX3
  • Solute carrier family 25 member 10
A0A0S2Z3G3
F6RGN5
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0060475 myoclonic-atonic epilepsy
DOID:0060536 mitochondrial complex I deficiency
DOID:0070329 mitochondrial DNA depletion syndrome
DOID:0070450 mitochondrial DNA depletion syndrome 19

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024